search
Back to results

Study of JS004 Combined With Toripalimab for Advanced Lung Cancer

Primary Purpose

Advanced Lung Cancer

Status
Recruiting
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
JS004 in combination with toripalimab
Sponsored by
Shanghai Junshi Bioscience Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Advanced Lung Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Sign the informed consent form voluntarily;
  2. Patient (both sex) ≥ 18 years at the time of signing informed consent;
  3. Expected survival ≥ 3 months;
  4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
  5. Extensive-stage small cell lung cancer (ES-SCLC, according to the Veterans Administration Lung Study Group VALG Staging) or/and locally advanced (stage IIIB/IIIC), metastatic or recurrent (stage IV) non-small cell lung cancer (NSCLC) by pathologically confirmed
  6. At least one measurable lesion as a target lesion (RECIST v1.1 criteria);
  7. Agree to provide tumor tissue samples (provide fresh biopsy samples before treatment as far as possible; provide archived samples within 2 years for patients who cannot provide fresh biopsy samples before treatment;
  8. The subject has good organ function as indicated by screening laboratory results
  9. Males of reproductive potential or females of childbearing potential must use effective contraceptive methods (such as oral contraceptives, intrauterine device or barrier method combined with spermicide) during the trial and continue contraception for 6 months after the end of treatment;
  10. Good compliance and cooperated with the follow-up.

Exclusion Criteria:

  1. Any malignancy other than the disease under study within the past 5 years, except for malignancies that can be expected to be cured after treatment (including but not limited to adequately treated thyroid cancer, carcinoma in situ of the cervix, basal or squamous cell skin cancer, or ductal carcinoma in situ of the breast treated surgically with curative intent);
  2. Patients previously treated with anti-BTLA or anti-HVEM antibodies;
  3. Patients previously discontinued treatment due to PD-1/PD-L1 inhibitor toxicity;
  4. Any adverse reactions caused by previous treatments have not recovered to CTCAE v5.0 Grade 1 or below (except alopecia and neurotoxicity, which cannot be recovered due to long-term presence as judged by the investigator);
  5. Received allogeneic hematopoietic stem cell transplantation or solid organ transplantation in the past;
  6. A large amount of hydrothorax or ascites or pericardial effusion with clinical symptoms or requiring symptomatic treatment;
  7. Pulmonary disease: interstitial pneumonia, obstructive pulmonary disease and symptomatic bronchospasm;
  8. Active infection requiring systemic therapy;
  9. A positive result for human immunodeficiency virus (HIV) antibody test;
  10. Known active tuberculosis (TB). For patients with suspicion of active TB should perform the test of chest X-ray, sputum, clinical signs and symptoms to exclude.
  11. Have a history of psychotropic drug abuse and unable to withdraw or have mental disorders;
  12. Pregnant or lactating woman;
  13. Known to be allergic to JS004 or toripalimab and its components;
  14. Other severe, acute or chronic medical or psychiatric disorders or laboratory abnormalities that, in the investigator's opinion, may increase the risk associated with study participation or may interfere with the interpretation of study results."

Sites / Locations

  • Jilin Cancer HospitalRecruiting
  • Cancer Hospital of Chinese Academy of Medical Sciences

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

JS004 200 mg in combination with toripalimab 240 mg was administered every 3 weeks as planned

Arm Description

Outcomes

Primary Outcome Measures

The incidence of adverse events (AE) and serious adverse events (SAE) were assessed
Incidence and severity of adverse events (AE) and serious adverse events (SAE) as assessed according to NCI-CTCAE 5.0, as well as abnormalities in vital signs, electrocardiogram, and laboratory tests

Secondary Outcome Measures

OS
Duration of Response
DOR
Duration of Response
DCR
Disease Control Rate
PFS
Progression-free survival
Cmax
Maximum Plasma Concentration
Tmax
Time to Cmax
AUC0-t
Area under the concentration versus time curve from time 0 to the last measurable concentration
AUC0-inf
AUC from time 0 to infinity
Kel
Elimination rate constant
t1/2
Elimination half life time
CL/F
Clearance
Vd/F
Apparent volume of distribution
Rac
Accumulation factor

Full Information

First Posted
August 10, 2021
Last Updated
September 5, 2021
Sponsor
Shanghai Junshi Bioscience Co., Ltd.
search

1. Study Identification

Unique Protocol Identification Number
NCT05000684
Brief Title
Study of JS004 Combined With Toripalimab for Advanced Lung Cancer
Official Title
A Phase I/II Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Initial Efficacy of Recombinant Humanized Anti-BTLA Monoclonal Antibody (JS004) Injection Combined With Toripalimab in Patients With Advanced Lung Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Recruiting
Study Start Date
August 27, 2021 (Actual)
Primary Completion Date
August 30, 2023 (Anticipated)
Study Completion Date
August 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Junshi Bioscience Co., Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This is an open-label phase I/II study to evaluate the safety, tolerability, pharmacokinetics and initial efficacy of JS004 injection combined with toripalimab in patients with advanced lung cancer who have failed standard therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Advanced Lung Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
66 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
JS004 200 mg in combination with toripalimab 240 mg was administered every 3 weeks as planned
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
JS004 in combination with toripalimab
Intervention Description
Usage and dosage: Inject 200mg once every 3 weeks
Primary Outcome Measure Information:
Title
The incidence of adverse events (AE) and serious adverse events (SAE) were assessed
Description
Incidence and severity of adverse events (AE) and serious adverse events (SAE) as assessed according to NCI-CTCAE 5.0, as well as abnormalities in vital signs, electrocardiogram, and laboratory tests
Time Frame
2 years
Secondary Outcome Measure Information:
Title
OS
Description
Duration of Response
Time Frame
2 years
Title
DOR
Description
Duration of Response
Time Frame
2 years
Title
DCR
Description
Disease Control Rate
Time Frame
2 years
Title
PFS
Description
Progression-free survival
Time Frame
2 years
Title
Cmax
Description
Maximum Plasma Concentration
Time Frame
2 years
Title
Tmax
Description
Time to Cmax
Time Frame
2 years
Title
AUC0-t
Description
Area under the concentration versus time curve from time 0 to the last measurable concentration
Time Frame
2 years
Title
AUC0-inf
Description
AUC from time 0 to infinity
Time Frame
2 years
Title
Kel
Description
Elimination rate constant
Time Frame
2 years
Title
t1/2
Description
Elimination half life time
Time Frame
2 years
Title
CL/F
Description
Clearance
Time Frame
2 years
Title
Vd/F
Description
Apparent volume of distribution
Time Frame
2 years
Title
Rac
Description
Accumulation factor
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Sign the informed consent form voluntarily; Patient (both sex) ≥ 18 years at the time of signing informed consent; Expected survival ≥ 3 months; Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1; Extensive-stage small cell lung cancer (ES-SCLC, according to the Veterans Administration Lung Study Group VALG Staging) or/and locally advanced (stage IIIB/IIIC), metastatic or recurrent (stage IV) non-small cell lung cancer (NSCLC) by pathologically confirmed At least one measurable lesion as a target lesion (RECIST v1.1 criteria); Agree to provide tumor tissue samples (provide fresh biopsy samples before treatment as far as possible; provide archived samples within 2 years for patients who cannot provide fresh biopsy samples before treatment; The subject has good organ function as indicated by screening laboratory results Males of reproductive potential or females of childbearing potential must use effective contraceptive methods (such as oral contraceptives, intrauterine device or barrier method combined with spermicide) during the trial and continue contraception for 6 months after the end of treatment; Good compliance and cooperated with the follow-up. Exclusion Criteria: Any malignancy other than the disease under study within the past 5 years, except for malignancies that can be expected to be cured after treatment (including but not limited to adequately treated thyroid cancer, carcinoma in situ of the cervix, basal or squamous cell skin cancer, or ductal carcinoma in situ of the breast treated surgically with curative intent); Patients previously treated with anti-BTLA or anti-HVEM antibodies; Patients previously discontinued treatment due to PD-1/PD-L1 inhibitor toxicity; Any adverse reactions caused by previous treatments have not recovered to CTCAE v5.0 Grade 1 or below (except alopecia and neurotoxicity, which cannot be recovered due to long-term presence as judged by the investigator); Received allogeneic hematopoietic stem cell transplantation or solid organ transplantation in the past; A large amount of hydrothorax or ascites or pericardial effusion with clinical symptoms or requiring symptomatic treatment; Pulmonary disease: interstitial pneumonia, obstructive pulmonary disease and symptomatic bronchospasm; Active infection requiring systemic therapy; A positive result for human immunodeficiency virus (HIV) antibody test; Known active tuberculosis (TB). For patients with suspicion of active TB should perform the test of chest X-ray, sputum, clinical signs and symptoms to exclude. Have a history of psychotropic drug abuse and unable to withdraw or have mental disorders; Pregnant or lactating woman; Known to be allergic to JS004 or toripalimab and its components; Other severe, acute or chronic medical or psychiatric disorders or laboratory abnormalities that, in the investigator's opinion, may increase the risk associated with study participation or may interfere with the interpretation of study results."
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaoyao Tian, MD
Phone
13514257836
Email
xiaoyao_tian@junshipharma.com
Facility Information:
Facility Name
Jilin Cancer Hospital
City
Changchun
State/Province
Jilin
ZIP/Postal Code
130012
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ying Cheng, Doctor
Phone
+8643180596067
Email
jl.cheng@163.com
Facility Name
Cancer Hospital of Chinese Academy of Medical Sciences
City
Beijing
ZIP/Postal Code
100029
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jie Wang, MD
Phone
13910704699
Email
zlhuxi@163.com

12. IPD Sharing Statement

Learn more about this trial

Study of JS004 Combined With Toripalimab for Advanced Lung Cancer

We'll reach out to this number within 24 hrs